Congenital hypofibrinogenemia.

dc.contributor.authorAwasthy, Neerajen_US
dc.contributor.authorAggarwal, K Cen_US
dc.contributor.authorGupta, Hen_US
dc.contributor.authorSaluja, Sen_US
dc.date.accessioned2004-02-09en_US
dc.date.accessioned2009-05-27T06:14:58Z
dc.date.available2004-02-09en_US
dc.date.available2009-05-27T06:14:58Z
dc.date.issued2004-02-09en_US
dc.description.abstractCongenital afibrinogenemia/hypofibrinogenemia is an extremely rare coagulation disorder. We describe a case of congenital hypofibrinogenemia in a 6-year female child, who presented with recurrent ecchymotic spots with no frank bleeding.en_US
dc.description.affiliationDepartment of Pediatrics, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi 110 029, India.en_US
dc.identifier.citationAwasthy N, Aggarwal KC, Gupta H, Saluja S. Congenital hypofibrinogenemia. Indian Pediatrics. 2004 Feb; 41(2): 185-7en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/15713
dc.language.isoengen_US
dc.source.urihttps://indianpediatrics.neten_US
dc.subject.meshAfibrinogenemia --complicationsen_US
dc.subject.meshBlood Coagulation Disorders --congenitalen_US
dc.subject.meshChilden_US
dc.subject.meshCombined Modality Therapyen_US
dc.subject.meshFemaleen_US
dc.subject.meshHemorrhage --etiologyen_US
dc.subject.meshHumansen_US
dc.subject.meshIndiaen_US
dc.subject.meshPrognosisen_US
dc.subject.meshRecurrenceen_US
dc.subject.meshSeverity of Illness Indexen_US
dc.titleCongenital hypofibrinogenemia.en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
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